Evolve your EDC approach and empower your clinical research with ShareCRF.

Smart electronic data capture software that let storage and manage clinical research data from multiple sources in one place easily.

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Every clinical research is unique.
Shape your solution flexibly, in days.

Creating data capture systems that meet specific study needs is challenging, and ensuring their user-friendliness is even harder. ShareCRF streamlines this complex process, making clinical research data management simpler and more efficient.

Adapt ShareCRF to any study type, from decentralized to traditional, ensuring versatile performance for diverse clinical research needs.

Visual Study Editor

Easily design clinical eCRF with our drag & drop editor. Without programming.

ePRO

Collect patient data directly from their devices, and integrate it automatically in the EDC along with other clinical data.

Randomization

Flexible, easy, integrated and with support for treatment stock management.

Medical Coding

Code on-the-go using MedDRA and  WHODrug: medical coding integrated with data.

DICOM & Big Files

Upload large files effortlessly, and with support for automatic anonymization to DICOM files.

API

Connects the EDC to other systems via our application programming interface.

Intuitive for every user: whether entering data or managing it, experience ease at every level.

In clinical trials, slow and unintuitive systems often lead to user frustration and operational inefficiencies, resulting in a cumbersome research process and jeopardized data quality. ShareCRF seamless addresses these challenges with its user-focused, intuitive, and streamlined design.

"The sites are very happy, because the ease of management, the speed of the system and the clarity, makes their work much easier and saves them time. They really like it."

Mercedes Ramas
Clinical Operations Header at QualitecFarma

"The most like of ShareCRF is the easy way to develop forms, it's very easy and with a very good flow to give a structure to the form."

Gabriela Jimenez
Medical Doctor at Picterus AS

"I think that all the users, from the studio coordinators to the monitor and myself, now the director/sponsor, enjoy the system very much. It's very easy to use. It's very intuitive and easy to use."

Sahar Boostenay
Clinical Director at Revamp Medical

"The graphical user interface for developing the eCRF is very intuitive. The most of our needs can be addressed without need for programming."

Iker Navarro
CEO at Noorik Biopharmaceuticals

"We found ShareCRF to be a better system in terms of ease of use, level of customer service and changes, and that interaction was very, very important to us."

Nicola Wall
CEO at Afortiori Development

"I think some solutions are more complicated, it means that the management of the creation of the CRF is not really easy and also there are some solutions which are really really more expensive and the functionalities are the same, so that is why we have chose ShareCRF"

Lenka Styfalova
Clinical Data Manager at Diabeloop

"when you have a eCRF that has to be explained in different sites, as in our last trial we had 12 sites, and you have an intuitive eCRF, that you don't have to explain how it works, you get the user who is going to use the eCRF to learn it with very little effort"

Javier Fernandez García
Project Manager at Clínica Universidad de Navarra

"the most like of ShareCRF is the user friendly access of the platform. We have 12  sites involved in the study and we had that feedback from investigators, and they all say the same that is straight forward to use"

Rita Carilho Torrao
Project Manager & Scientific Affairs at AIDFM-CETERA

Clinical Data Management Superpowers.
Get more done, quicker and with less effort.

Overcome complex and repetitive challenges of clinical data management. ShareCRF’s cutting-edge automation handles the complexities, ensuring a smoother trial process.

Quick initial setup

Quickly set up your study with our intuitive drag & drop Visual Study Editor, no coding required. Reuse previous study designs, benefit from auto-generated documents (annotated CRF  & blank CRF), and manage multiple CRF versions effortlessly, reducing time spent on data reconciliation.

Easy Mid-Study Changes

Make mid-study changes easily with our EDC: use our secure test environment, to validate changes before publishing them, and when the changes are ready publish the new version (without having to pause the study) at the touch of a button. All this while maintaining data security and integrity.

Get High Quality Data

Achieve high-quality data with our EDC: dynamic validation ensures real-time consistency, automated reminders boost user engagement and data accuracy, and our flexible monitoring system allows you to tailor data review workflows to the needs of each study.

Efficient Trial Oversight

Improve control over your clinical trial with customizable notifications that allow you to stay informed of key events. Our reporting module provides intuitive visualizations of key metrics, allowing you to make data-driven decisions for better outcomes in your clinical trials.

Customer Support That Truly Assists – No Hassles, Just Solutions.

In clinical research, swift and accurate support is crucial. ShareCRF stands apart with its in-house specialized technical team, providing precise, expert solutions right from the first interaction. No endless back-and-forth, just professional answers that keep your research moving forward.

"The level of support service has been wonderful, and the capabilities of the ShareCRF team and the ability to work really well with our team"

Nicola Wall
CEO at Afortiori

"The main benefit of ShareCRF, apart from the obvious ease of use, is the speed of response to any problem."

Mercedes Ramas
Clinical Operations Manager at QualitecFarma

“I always received the most professional and immediate response by the customer service team. They offered solutions that I couldn't even think of, which was amazing.”

Sahar Boostenay
Clinical Director at Revamp Medical

“Customer support team is very, very fast responding, and always responding what I needed to know”

Gabriela Jimenez
Medical Doctor at Picterus AS

“The support team has been extremely responsive, very precise in their answers, and we feel that the tool is mature.”

Iker Navarro
CEO at Noorik Biopharmaceuticals

“The two best things of ShareCRF are the quick and in depth customer support, and it is the fact that is so easy to modify on the fly. It's really good.”

Anjali Raja
Co-Founder at Collabree

“The support has been what we would expect. It is effective, it is not time consuming, we usually get a straight answer and in really quick period of time.”

Rita Carilho
Project Manager & Scientific Affairs at AIDFM-CETERA

“Very good communication with the assistance team, highly responsive to all our requests and study needs. great user experience.”

Iris Yadin
Clinical Development Manager at Cardiac Success

“The system is very easy to use and the customer service is very good.”

Steven Roney
Clinical Research Associate at Afortiori

Compliance Made Simple

Leverage ShareCRF to meet complex regulatory requirements in the simplest way. Designed to facilitate compliance with legal and regulatory standards. ShareCRF is validated using the GAMP5 methodology.

  • Validated System (GAMP5)
  • 21 CFR Part 11 (FDA)
  • Annex 11: Computerised Systems (EMA)
  • ISO 9001 certified
  • GDPR
  • ICH E6 (R2) - Good Clinical Practice
  • HIPAA
  • ISO 27001 certified
  • GDPR
  • ICH E6 (R2) - Good Clinical Practice
  • HIPAA
  • ISO 27001 certified

Success Stories

“ It's a very easy, simple user friendly system, affordable, pricewise and the professional service provided by the support or by the design team is, is amazing”

Sahar Boostenay
Clinical Director at Revamp Medical

"What I like most about ShareCRF is the independence and also the functionalities, which are really sophisticated."

Lenka Styfalova
Clinical Data Manager at Diabeloop

“The designing process is quite easy, and we can customise the form to our needs. And also thinking about the researchers that use this tool, I think for them is very easy. One of the benefits is that it eases the work a lot both for us and for the users.”

Gabriela Jimenez
Medical Doctor at Picterus AS

“I would have used other very large well known systems, but actually, there were just a number of different issues that did not make those systems suitable for the type of CRO that we were trying to run. We were definitely looking for a better system in terms of ease of use, level of customer service and changes and that interaction was very, very important to us and price actually as well”

Nicola Wall
CEO at Afortiori

“If a company is in the need to develop quick collect data forms that comply with regulatory requirements, this is an ideal solution. You can develop complex tools quickly.”

Iker Navarro
CEO at Noorik Biopharmaceuticals

“The major benefit would be time, lots of time saving. It is easy to introduce the data and it's really fast to export the data and from that on to analyse the data obtained in the studies.”

Rita Carilho
Project Manager & Scientific Affairs at AIDFM-CETERA

“The fact that I can design the eCRF by myself, I realised it is really helpful because I can modify all the time, like when I need and I think it is a huge benefit”

Anjali Raja
Co-Founder at Collabree

They already trust in ShareCRF

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ShareCRF in numbers

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5.000
Users
+
600
Studies
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65
Countries
99.99
%
Availability